Mosaicism of the UDP-Galactose Transporter SLC35A2 Causes a Congenital Disorder of Glycosylation-Reference-Cited by-同舟云学术

Mosaicism of the UDP-Galactose Transporter SLC35A2 Causes a Congenital Disorder of Glycosylation

Published:2013-04 Issue:4 Volume:92 Page:632-636
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ng Bobby G.,Buckingham Kati J.,Raymond Kimiyo,Kircher Martin,Turner Emily H.,He Miao,Smith Joshua D.,Eroshkin Alexey,Szybowska Marta,Losfeld Marie E.,Chong Jessica X.,Kozenko Mariya,Li Chumei,Patterson Marc C.,Gilbert Rodney D.,Nickerson Deborah A.,Shendure Jay,Bamshad Michael J.,Freeze Hudson H.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference11 articles.

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4. Genetic defects in the human glycome;Freeze;Nat. Rev. Genet.,2006

5. Comparative analysis of involvement of UGT1 and UGT2 splice variants of UDP-galactose transporter in glycosylation of macromolecules in MDCK and CHO cell lines;Maszczak-Seneczko;Glycoconj. J.,2011

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